FDA.reportPublic FDA data

141010 HYDROQUINONE 4%

Manufacturer
Sincerus Florida, LLC
Effective date
2020-07-02
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 20:33:01

Label at a glance#

Product141010 HYDROQUINONE 4%
Active ingredientHYDROQUINONE
Label structure4 sections

Label contents#

Full prescribing information#

Directions for use

INSTRUCTIONS FOR USE SECTION

ss

Sincerus Florida, LLC adverse reactions

ADVERSE REACTIONS SECTION

dd

Active, incative

COMPONENTS

ss

NDC 72934-6223-2 141010 HYDROQUINONE 4% Emulsion 30 gm

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ss

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
HYDROQUINONE Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
85490a6b-2306-6bf2-c51b-eb63537dc2daProduct name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72934-6223-22022-01-28C16284748780-1d6a99b39-a9c2-a426-e053-dadaa90af4c2141010 HYDROQUINONE 4%

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72934-6223-2141010 HYDROQUINONE 4%30 g in 1 BOTTLE, PUMPEMULSION301

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72934-6223141010 HYDROQUINONE 4% EMULSION [SINCERUS FLORIDA, LLC]1Legacy NDC, 1 package rows20200703_a9799d58-35f7-c981-e053-2a95a90a0871.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 2 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72934-622372934-6223-2

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 1 matching rows.

Name, UNII, Kind table
NameUNIIKind
HYDROQUINONEXV74C1N1AEACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
a9799d58-35f8-c981-e053-2a95a90a0871a9799d58-35f7-c981-e053-2a95a90a08712020-07-02Adverse reactionsExact identifier
spl id: a9799d58-35f8-c981-e053-2a95a90a0871
spl set id: a9799d58-35f7-c981-e053-2a95a90a0871

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.